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放大并反转不对称光聚合反应中的手性偏向

Amplifying and Reversing the Chiral Bias in Asymmetric Photo-Polymerization Reaction.

作者信息

Liu Dingdong, Xu Xiangxiang, Feng Zeyu, Zhang Chutian, Li Jialei, Xie Yifan, Li Jingguo, Zhang Hongli, Zou Gang

机构信息

Key Laboratory of Precision and Intelligent Chemistry, School of Chemistry and Materials Science, University of Science and Technology of China, Hefei, Anhui, 230026, China.

CAS Key Laboratory of Urban Pollutant Conversion, Department of Environmental Science and Engineering, University of Science and Technology of China, Hefei, Anhui, 230026, China.

出版信息

Adv Sci (Weinh). 2025 Feb;12(5):e2411439. doi: 10.1002/advs.202411439. Epub 2024 Dec 12.

Abstract

Circularly polarized light (CPL) is inherently chiral and is regarded as one possible source for the origin of homochirality. Coincidentally, chiral metal nanoparticles have great prospects in asymmetric photochemical reactions since they can enhance the chiral light-matter interactions. Nonetheless, little is known about how the spin angular momentum of light competes with the chiral electromagnetic field in the vicinity of a chiral nanoparticle during the chiral induction and amplification process. Here, an asymmetric photo-polymerization system is presented where the chiral bias can be selectively regulated by the combination of chiral fields CPL and Ag nanoparticles, either constructively or destructively. Synergistic chiral amplification effect is observed when the handedness of both are matched, while the opposite-handed CPL can overrule the polymer helicity during the chain propagation process when the chiral near-field is weak. There is a bifurcation point in the chiral bias for the orthogonal control of the polymer helicity during the asymmetric photo-polymerization process, favoring for programmable chiroptical micropatterns and multi-channel independent information encoding. This work not only highlights opportunities for selectively regulating the asymmetric photopolymerization but also is highly valuable for fundamental understanding of the symmetry breaking in photochemical reactions.

摘要

圆偏振光(CPL)本质上具有手性,被视为同手性起源的一种可能来源。巧合的是,手性金属纳米颗粒在不对称光化学反应中具有广阔前景,因为它们可以增强手性光与物质的相互作用。然而,在 chiral 诱导和放大过程中,关于光的自旋角动量如何与手性纳米颗粒附近的手性电磁场竞争,人们所知甚少。在此,提出了一种不对称光聚合系统,其中手性偏置可以通过手性场CPL和银纳米颗粒的组合进行选择性调节,无论是建设性的还是破坏性的。当两者的手性匹配时,观察到协同手性放大效应,而当手性近场较弱时,相反手性的CPL可以在链增长过程中推翻聚合物的螺旋度。在不对称光聚合过程中,聚合物螺旋度的正交控制在手性偏置方面存在一个分岔点,有利于可编程的手性光学微图案和多通道独立信息编码。这项工作不仅突出了选择性调节不对称光聚合的机会,而且对于光化学反应中对称性破缺的基本理解也具有很高的价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f1f/11792003/d756a13785d4/ADVS-12-2411439-g004.jpg

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